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Volumn 132, Issue 6, 2010, Pages 1798-1799

Nontraditional reactions of azomethine ylides: Decarboxylative three-component couplings of α-amino acids

Author keywords

[No Author keywords available]

Indexed keywords

AZOMETHINE YLIDES; DIPOLAROPHILES; IN-SITU; NITROALKANES; THREE-COMPONENT COUPLING;

EID: 77249123927     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja910719x     Document Type: Article
Times cited : (198)

References (47)
  • 9
    • 0039338892 scopus 로고
    • For selected reviews, see: (a) Padwa, A, Ed, Wiley: New York, NY
    • For selected reviews, see: (a) Padwa, A., Ed. 1,3-Dipolar Cycloaddition Chemistry, Vol. 1; Wiley: New York, NY, 1984; p 817.
    • (1984) 1,3-Dipolar Cycloaddition Chemistry , vol.1 , pp. 817
  • 10
    • 84910004125 scopus 로고
    • Padwa, A, Ed, Wiley: New York, NY
    • (b) Padwa, A., Ed. 1,3-Dipolar Cycloaddition Chemistry, Vol. 2.; Wiley: New York, NY, 1984; p 704.
    • (1984) 1,3-Dipolar Cycloaddition Chemistry , vol.2 , pp. 704
  • 15
    • 0002845373 scopus 로고    scopus 로고
    • Azomethine ylides are known to engage in 1,5- or 1,7-electrocyclizations: (a) Arany, A.; Bendell, D.; Groundwater, P. W.; Garnett, I.; Nyerges, M. J. Chem. Soc., Perkin Trans. 1999, 1, 2605.
    • Azomethine ylides are known to engage in 1,5- or 1,7-electrocyclizations: (a) Arany, A.; Bendell, D.; Groundwater, P. W.; Garnett, I.; Nyerges, M. J. Chem. Soc., Perkin Trans. 1999, 1, 2605.
  • 26
    • 0037174448 scopus 로고    scopus 로고
    • Metal catalyzed decarboxylative couplings have recently emerged as valuable synthetic tools. For examples, see: a
    • Metal catalyzed decarboxylative couplings have recently emerged as valuable synthetic tools. For examples, see: (a) Myers, A. G.; Tanaka, D.; Mannion, M. R. J. Am. Chem. Soc. 2002, 124, 11250.
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 11250
    • Myers, A.G.1    Tanaka, D.2    Mannion, M.R.3
  • 43
    • 34250769398 scopus 로고    scopus 로고
    • For an excellent review on the R-functionalization of amines, see
    • For an excellent review on the R-functionalization of amines, see: Campos, K. R. Chem. Soc. Rev. 2007, 36, 1069.
    • (2007) Chem. Soc. Rev , vol.36 , pp. 1069
    • Campos, K.R.1
  • 46
    • 75749123474 scopus 로고    scopus 로고
    • After the submission of this manuscript, the formation of products 8 under similar conditions was reported: Bi, H.-P.; Teng, Q.; Guan, M.; Chen, W.-W.; Liang, Y.-M.; Yao, X.; Li, C.-J. J. Org. Chem. 2010 (DOI: 10.1021/ jo902319h).
    • After the submission of this manuscript, the formation of products 8 under similar conditions was reported: Bi, H.-P.; Teng, Q.; Guan, M.; Chen, W.-W.; Liang, Y.-M.; Yao, X.; Li, C.-J. J. Org. Chem. 2010 (DOI: 10.1021/ jo902319h).
  • 47
    • 77249156368 scopus 로고    scopus 로고
    • The use of lower amounts of benzoic acid gave rise to lower yields
    • The use of lower amounts of benzoic acid gave rise to lower yields.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.